Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,160 recalls have been distributed to Arizona in the last 12 months.
Showing 2141–2160 of 29,154 recalls
Recalled Item: Medline procedure kits labeled as: 1) ABLATION PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS Software Version 7.4.x Recalled by FUJIFILM Healthcare Americas...
The Issue: The incorrect computed patient age is showing in VX for patients less than 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ACOUSTIC NEUROMA PACK-LF Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) AV FISTULA PACK-LF Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) LACERATION TRAY Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT Recalled by...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline procedure kits labeled as: 1) EYE PACK Recalled by MEDLINE...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candida ID Antigen Recalled by Immuno-Mycologics, Inc Due to Candida...
The Issue: Candida Immunodiffusion Antigen may have reduced sensitivity which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Pak with Non-Latex Symbol Recalled by Alcon Research LLC Due to...
The Issue: Customer-designed sterile surgical procedure packs contain latex components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origin Data Management software versions 3.1.0 Recalled by Brainlab AG Due...
The Issue: Under certain circumstances, it can occur that patient records from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial...
The Issue: Damage to the sterile barrier pouch of catheter, which could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LABOR & DELIVERY PPS Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR DIULUS INJECTION PACK Recalled by American Contract Systems Inc Due to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENERAL LAPAROSCOPIC PACK-LF Recalled by American Contract Systems Inc Due...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIP SCOPE Recalled by American Contract Systems Inc Due to ACS is unable to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENERAL ANGIO PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: Beckman Coulter identified that an issue for DxI 9000 tip stocker interface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.